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Perillen

$576

  • Brand : BIOFRON

  • Catalogue Number : BD-D1375

  • Specification : 98%(HPLC)

  • CAS number : 539-52-6

  • Formula : C10H14O

  • Molecular Weight : 150.22

  • PUBCHEM ID : 68316

  • Volume : 0.1ML

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Catalogue Number

BD-D1375

Analysis Method

HPLC,NMR,MS

Specification

98%(HPLC)

Storage

-20℃

Molecular Weight

150.22

Appearance

White crystalline powder

Botanical Source

Erilla frutescens (L.) Britt./oil of Perilla citriodora. Defence substance from Lasius fulginosus and Liothrips spp.

Structure Type

Alkaloids

Category

Standards;Natural Pytochemical;API

SMILES

CC(=CCCC1=COC=C1)C

Synonyms

Perillene/Perillen/3-(4-Methyl-3-pentenyl)furan/3-(4-Methyl-3-penten-1-yl)furan/Furan, 3-(4-methyl-3-penten-1-yl)-/3-(4-Methylpent-3-en-1-yl)furan

IUPAC Name

3-(4-methylpent-3-enyl)furan

Applications

Density

0.9±0.1 g/cm3

Solubility

Methanol; Ethanol; Chloroform; Petroleum ether

Flash Point

55.9±5.6 °C

Boiling Point

185.5±9.0 °C at 760 mmHg

Melting Point

InChl

InChI=1S/C10H14O/c1-9(2)4-3-5-10-6-7-11-8-10/h4,6-8H,3,5H2,1-2H3

InChl Key

XNGKCOFXDHYSGR-UHFFFAOYSA-N

WGK Germany

RID/ADR

HS Code Reference

2932190000

Personal Projective Equipment

Correct Usage

For Reference Standard and R&D, Not for Human Use Directly.

Meta Tag

provides coniferyl ferulate(CAS#:539-52-6) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Articles of coniferyl ferulate are included as well.>> amp version: coniferyl ferulate

No Technical Documents Available For This Product.

PMID

18196236

Abstract

The conversion of beta-myrcene to the furanoid flavour compound perillene by Pleurotus ostreatus was investigated using trideutero beta-myrcene, trideutero alpha-(Z)-acaridiol and non-labeled 1,2- and 3,10-epoxy-beta-myrcene, alpha,alpha-acarilactol, and perillene as substrates. Myrcene diols were formed from the cleavage of myrcene epoxides, but only alpha-(Z)-acaridiol, a 1,4-butanediol derivative most likely generated through a base-catalysed epoxide opening, was a suitable precursor of perillene. Once formed, this key intermediate was rapidly oxidised and the resulting cyclic lactol was dehydrated to yield perillene. Bioconversion of the supplemented perillene to alpha,alpha-acariolide indicated that perillene was another intermediate of the pathway and prone to further oxidative degradation. The data suggest that the fungus converted the cytotoxic beta-myrcene in its environment into a metabolically useable carbon source along this route.

Title

A labeling study on the formation of perillene by submerged cultured oyster mushroom, Pleurotus ostreatus.

Author

Krings U1, Hapetta D, Berger RG.

Publish date

2008 Mar